Nature | Vol 577 | 16 January 2020 | 393analysis, and comparison to scRNA-seq data from adult trigeminal
ganglia (see Methods, Extended Data Figs. 2a, b, 3a–d, Supplementary
Data 1). These cell-type classifications are consistent with previously
published RNA-seq findings of adult DRG and trigeminal ganglia^16 –^19.
We next sought to determine how the transcriptional identities of
mature somatosensory neuron subtypes compare to those of newborn
sensory neurons by analysing the transcriptomes of cells from DRG at
E11.5 (Fig. 1b). We visualized the E11.5 scRNA-seq data using uniform
manifold approximation and projection (UMAP)^20. Mapping historically
defined marker genes onto the UMAP representation revealed three
principal cell types in E11.5 ganglia: 1) multipotent neural crest progeni-
tors (NCPs), marked by Sox10^21 ,^22 ; 2) sensory neuron progenitors (SNPs),
marked by Neurog1 and Neurog2^23 ; and 3) nascent, postmitotic sensory
neurons marked by expression of the somatosensory neuron gene advil-
lin (Avil^24 ) and concomitant loss of expression of cell-cycle-associated
genes (Fig. 1b, Extended Data Fig. 4a). Monocle 3^25 was then used to infer
developmental relationships between NCPs, SNPs, and nascent Avil+
sensory neurons. This analysis revealed a single continuous trajectory
connecting NCPs, SNPs, and Avil+ sensory neurons, suggesting a lack
of transcriptional diversity in sensory neuron progenitors populating
the Avil+ compartment. Unexpectedly, labelled descendants of Neu-
rog1+ SNPs from Neurog1Cre; Rosa26LSL-tdTomato mice had a broad range
of cell diameters (Fig. 1c), consistent with the previous finding that
in vitro directed differentiation with Neurog1 overexpression leads to
the generation of both small- and large-diameter DRG sensory neuron
subtypes^26. Moreover, genes that were highly enriched in E11.5 Avil+
sensory neurons, relative to progenitors, generally remained expressed
in adult somatosensory neuron subtypes (Extended Data Fig. 4b). On
the other hand, the majority of genes whose expression was restricted
to individual terminal somatosensory subtypes of adult ganglia were
expressed at trace levels in E11.5 Avil+ sensory neurons (Fig. 1d), sug-
gesting that upon cell-cycle exit sensory neurons are transcriptionallyPostnatal day 5SSTMRGPRD+
ProprioceptorsAβ RA-LTMRAβ eld/SA1C-LTMR
CGRP-α
CGRP-ε
CGRP-η
CGRP-γCGRP-θ
CGRP-ζCold thermoceptors
Unassigned/
non-neuronalAδ-LTMRSST
CGRP-θAδ-LTMRC-LT MRAβ RA- LTM
R
ProprioceptorsCGRP-α
CGRP-γCGRP-η
CGRP-CGRP-ζ εAβ
eld/SA1Cold
thermoceptorsMRGPRD+ polymodal
nociceptorsCold
thermoceptors
CGRP-αCGRP-γCGRP-ηC-LTMRMRGPRD+ polymodal
nociceptors
SST
CGRP-θCGRP-ε
CGRP-ζ
Aβ eld/SA1Aδ-LTMR
Aβ RA-LTMRProprioceptorsPropr
ioceptorsAδ-L
TMR
C-LTMRMRGPRD
+ thermo.ColdCGRP-CGRP-α
θCGRP-
εCGRP-
ζAβ RA-L
TMRAβ eld/SA1CGRP-ηAdult Postnatal day 0Embryonic day 15.5 Embryonic day 12.5aNeural crest progenitor
Unspecialized sensory neuronNeural crest progenitors
(Sox10)02Unspecialized sensory neurons
(Avil)01ln(TPT+1)Embryonic day 11.5ln(TPT+1)Sensory neuron progenitors
(Neurog1)03ln(TPT+1)Sensory neuron progenitor
Inferred trajectoryInferred trajectory tdTomato tdTNeuNomato^75 μmNeurog1Cre/WT;Rosa26LSL-tdTomato/WT100tdT 0omato+neurons (%)<20μm
20–30μm
>30μmb cdAβ eld/SA1Aβ (^) RA-L
TMR
Aδ-LTMR
CGRP-α C-LTMR
CGRP-ε CGRP-η
CGRP-θ CGRP-γ
CGRP-ζ
MRGPRD+ polymodal
nociceptors
Proprioceptors
SST+
Cold
thermoceptors
Non-neuronal
SST
Aβ RA-LTMR
MRGPRD+ polymodal
nociceptors
C-LT MR
CGRP-θ
CGRP-γCGRP-ε
CGRP-ζ
Aδ-LTMR
Aβ eld/SA1Proprioceptors
CGRP-η
Cold
thermoceptors
CGRP-α
Adult
Aβ eld/SA1Aβ RA-LTMR
Adult
Aδ-LTMR
Adult
C-LTMR
Adult Adult
0.5 0.6
CGRP-α CGRP-ε CGRP-η
CGRP-γ CGRP-θ CGRP-ζ MRGPRD+ Proprioceptors SST Cold thermo.
0.4 0.6
0.6 0.4 0.6
- 0.6
0.4 0.6
0.6 0.8
- 0.8 0.6
ln(TPT+1) *
Cell-type-
specic genes
Cells
ln(TPT+1)
0 0 0 0 0 0 0
0 0 0 0 0 0 0
Adult Adult
0
2
ln(TPT+1)
USNUSN USN USNUSN USN USN
USNUAdult SNAdultUSNUAdult SNAdultUSNAdult USNUAdult SNAdult
- 0.8 0.6
NCP
Neuron
(cell state)
Neurog1(Genetic strategy)Cre/WTSNP
;Rosa26
LSL-tdTomato
/WT
Fig. 1 | scRNA-seq of developing and mature DRG sensory neurons. a, t-SNE
visualizations of DRG scRNA-seq data. SST, somatostatin. b, UMAP
visualization of DRG scRNA-seq data from E11.5 with developmental trajectory
and gene expression information overlaid. TPT, tags per ten thousand.
c, Quantification (mean ± s.e.m.) of tdTomato+ neurons and representative
image (right). d, Heat map and quantification of genes enriched in each
somatosensory neuron subtype as well as their expression levels in
unspecialized sensory neurons (USNs). Boxes represent interquartile range
(IQR), whiskers represent minimum and maximum values, and notches
represent the 95% confidence interval of the median. *P < 0.0001, two-sided
Wilcoxon rank-sum test with Bonferroni correction. For n values, see Methods.